Javascript must be enabled to continue!
Abstract 1558: Drug repurposing strategies for pancreatic cancer management
View through CrossRef
Abstract
Pancreatic ductal adenocarcinoma (PDAC) is the currently the third leading cause of cancer related deaths and is projected to be the second leading cause by 2030. The difficulty in diagnosis and aggressiveness of the disease makes it a difficult-to-treat cancer. Currently, treatment of PDAC mainly involves use of standard chemotherapeutic combinations. Although effective, the current options do not always provide a benefit and patients develop resistance over time. Additionally, the adverse effect profile of standard regimen is a concern. Thus, novel agents which offer better clinical and survival response are urgently required. Drug repurposing is an effective strategy to overcome the limitations in current treatment options. Through drug repurposing, we identified the anti-cancer effects of a compound MBO in human PDAC cell lines AsPC-1, MiaPaCa-2, BXPC3, Panc-1 and SUIT-2. Further, we observed the ability of MBO to suppress colony formation in PDAC cell lines AsPC-1, MiaPaCa-2 and BXPC3. Additionally, MBO induced cell death by apoptosis in PDAC cell lines which was confirmed by Annexin V/FITC analysis using flow cytometry. MBO significantly suppressed tumor growth in a subcutaneous model of PDAC. Studies are currently ongoing to explore the mechanism of action as well as effect of MBO in orthotopic PDAC models.
Citation Format: Shreyas R. Gaikwad, Sanjay K. Srivastava. Drug repurposing strategies for pancreatic cancer management [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2022; 2022 Apr 8-13. Philadelphia (PA): AACR; Cancer Res 2022;82(12_Suppl):Abstract nr 1558.
American Association for Cancer Research (AACR)
Title: Abstract 1558: Drug repurposing strategies for pancreatic cancer management
Description:
Abstract
Pancreatic ductal adenocarcinoma (PDAC) is the currently the third leading cause of cancer related deaths and is projected to be the second leading cause by 2030.
The difficulty in diagnosis and aggressiveness of the disease makes it a difficult-to-treat cancer.
Currently, treatment of PDAC mainly involves use of standard chemotherapeutic combinations.
Although effective, the current options do not always provide a benefit and patients develop resistance over time.
Additionally, the adverse effect profile of standard regimen is a concern.
Thus, novel agents which offer better clinical and survival response are urgently required.
Drug repurposing is an effective strategy to overcome the limitations in current treatment options.
Through drug repurposing, we identified the anti-cancer effects of a compound MBO in human PDAC cell lines AsPC-1, MiaPaCa-2, BXPC3, Panc-1 and SUIT-2.
Further, we observed the ability of MBO to suppress colony formation in PDAC cell lines AsPC-1, MiaPaCa-2 and BXPC3.
Additionally, MBO induced cell death by apoptosis in PDAC cell lines which was confirmed by Annexin V/FITC analysis using flow cytometry.
MBO significantly suppressed tumor growth in a subcutaneous model of PDAC.
Studies are currently ongoing to explore the mechanism of action as well as effect of MBO in orthotopic PDAC models.
Citation Format: Shreyas R.
Gaikwad, Sanjay K.
Srivastava.
Drug repurposing strategies for pancreatic cancer management [abstract].
In: Proceedings of the American Association for Cancer Research Annual Meeting 2022; 2022 Apr 8-13.
Philadelphia (PA): AACR; Cancer Res 2022;82(12_Suppl):Abstract nr 1558.
Related Results
High Expression of AMIGO2 Is an Independent Predictor of Poor Prognosis in Pancreatic Cancer
High Expression of AMIGO2 Is an Independent Predictor of Poor Prognosis in Pancreatic Cancer
Abstract
Background.The AMIGO2 extracellular domain has a leucine - rich repetitive domain (LRR) and encodes a type 1 transmembrane protein , and is a member of the AMIGO g...
Abstract 1603: Intra-pancreatic fat promotes the progression of PDAC by activating thermogenesis
Abstract 1603: Intra-pancreatic fat promotes the progression of PDAC by activating thermogenesis
Abstract
Background: The presence of minimal intra-pancreatic fat deposition (IPFD) in the healthy human pancreas has been demonstrated in numerous studies. But exce...
High KLK7 Expression Predicts Unfavorable Outcomes in Patients with Resectable Pancreatic Ductal Adenocarcinoma
High KLK7 Expression Predicts Unfavorable Outcomes in Patients with Resectable Pancreatic Ductal Adenocarcinoma
Abstract
Background Studies have shown that kallikrein-related peptidase 7 (KLK7) is abnormally expressed in a various of tumours and plays a crucial role in tumour progres...
Multiscale virtual screening optimization for shotgun drug repurposing using the CANDO platform
Multiscale virtual screening optimization for shotgun drug repurposing using the CANDO platform
Abstract
Drug repurposing, the practice of utilizing existing drugs for novel clinical indications, has tremendous potential for improving human health outcomes and...
The Dual Effects of Silibinin on Human Pancreatic Cells
The Dual Effects of Silibinin on Human Pancreatic Cells
Objective: Silibinin is a flavonoid with antihepatotoxic properties, and exhibits pleiotropic anticancer effects. However, the molecular mechanisms responsible for its anticancer a...
Abstract A044: Persistence of fetal splanchnic gene signature defines a tumor-restraining fibroblast subtype in pancreatic cancer
Abstract A044: Persistence of fetal splanchnic gene signature defines a tumor-restraining fibroblast subtype in pancreatic cancer
Abstract
The pancreas is composed of the epithelial and mesenchymal cells. While mesenchymal fibroblasts are a minor component of the normal pancreas, fibroblast pop...
Activated Pancreatic Stellate Cells Enhance the Warburg Effect to Cause the Malignant Development in Chronic Pancreatitis
Activated Pancreatic Stellate Cells Enhance the Warburg Effect to Cause the Malignant Development in Chronic Pancreatitis
Abstract
Background: Chronic pancreatitis (CP) is a precancerous condition associated with pancreatic ductal adenocarcinoma (PDAC), but its evolutionary mechanism is unclea...
Abstract 1814: Novel ABC transport inhibitor as a treatment for pancreatic and prostate cancers
Abstract 1814: Novel ABC transport inhibitor as a treatment for pancreatic and prostate cancers
Abstract
ABC transporters are the active transport systems of the cell involved in the export or import of a wide variety of molecules. We discovered that a member o...

